A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980795



Internal ID12972009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19143865..19538365hg38UCSC Ensembl
Innerchr10:19432794..19827294hg19UCSC Ensembl
Innerchr10:19472800..19867300hg18UCSC Ensembl
Innerchr10:19472800..19867300hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38394501
hg19394501
hg18394501
hg17394501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750886
Supporting Variants
SamplesBEC_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980795
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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